Your specialist in Quality and Compliance Management within Life Science.

The complex rules of our regulated industry are changing constantly. Your business needs to keep up with that change to be compliant, and deliver quality. Let us guide you.

About

About Q-people

Q-People provides targeted solutions in Quality and Compliance projects in the Life Sciences sector, from Pharmaceutical and Biotech to API and Medical Device Production.

About our company

Q-Expertise

What we do

Q-People helps companies to set up and support Quality and Compliance processes, procedures and systems. Training, mentoring and coaching of talent within the Life Sciences sector is our strength. We don’t want specialist knowledge or talent to go to waste.

we design

Every quality process requires an approach tailored to the specific needs of the production environment. We map out the current situation in accordance with the latest legislation.

we execute

Through validation and controlling quality risks we guarantee that your company complies with regulations and product safety is guaranteed.

we train

Training, mentoring and coaching, not only of our own consultants, and your talented staff is our strength.

client testimonials

meet our satisfied customers

In our daily rush we sometimes lose sight of what management is all about: creating the best team for the job at hand. Therefore, this focus-group was a nice and pleasant opportunity to focus on this topic.

Continuous improvement requires competent people come together and share their thoughts. Thanks to Q-People to make this happen.

Client testimonials

Design and development of quality management systems
Assistance in defining compliancy strategies
Validation Processes, software and equipment
Control of quality risks
Preparation of quality and compliance audits

Are educated and committed people who will bring added-value
Have a background in the Life Sciences sector
Are uniquely skilled, to cover the Full Quality Management System
Will continuously be trained and certified
Guarantee a powerful level of engagement

Q-people Testimonials

Meet our Q-Experts

They stimulate you to achieve your professional goals.

From the first contact, I felt that Q-People gives special attention to its employees. I was assisted throughout the search for a new project, until I started at the customer.

At Q-People they always take my expectations and feelings into account when they propose a mission.

The trademark of Q-People is to ensure your well-being and the professional development of its human resources.

As a consultant for Q-People I notice that the support from the back-office and the introduced trainings are contributing to my evolution and this is a positive experience as well for me as for the client.

Meet our q-experts

Our stories

Latest News

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Q-Academy training: Behandelen en technisch schrijven van deviaties

Volgende opleiding op maandag 9 december, Behandelen en technisch schrijven van deviaties, gaat door in het Darwin wetenschapspark te Niel. Deze opleiding binnen onze Q-Academy zijn "gratis" beschikbaar via Co-valent: Co-valent biedt GRATIS opleidingen aan voor ondernemingen die behoren tot de life science sector - paritair comité 116 (arbeiders) of 207 (bedienden). Deviaties (=afwijkingen) en CAPA’s blijven een belangrijk agendapunt tijdens audits. Voor professionals met beperkte ervaring of nieuw in de farmaceutische industrie vraagt dit een goede kennis en enige ervaring om GMP verdedigbare documentatie op te stellen. Deze opleiding geeft een goed overzicht van hoe deviaties opgevolgd, onderzocht & gedocumenteerd kunnen worden. Gezien het belang van de gestructureerde manier van documentatie en de juiste bewoording, geven we in deze opleiding het meeste aandacht aan de juiste schrijfmethodologie. Schrijf je hier snel want de plaatsen zijn beperkt: https://www.co-valent.be/nl/details-formations/?sja=704fadd0Zb278Ze911Za96aZ000d3a29f080

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Fundamentals in Validation: Equipment & System Qualification

Er zijn nog enkele plaatsen vrij voor onze uitgebreide training "Basics in Validatie". Deze 2 dagen gaan we van de basis naar tips en tricks om op een hoger niveau te komen binnen de validatie. Al de sessies van onze Q-Academy worden via Co-Valent verzorgt in het Darwin wetenschapspark te Niel. DAG 1: Voor professionals die nieuw zijn in de (bio-)farmaceutische of biomedische industrie, legt deze training uit waarom regulatorische autoriteiten validatie verwachten. Bovendien worden de mogelijke gevolgen van niet – of foutief gevalideerde processen of systemen besproken. Voor meer details DAG 1: https://www.co-valent.be/nl/details-formations/?sja=b9ef8c5dZfd5fZe811Zba26Z005056b04a46 Dag 2: Voor meer ervaren professionals gaan we dieper in op de details, pitfalls en mogelijke tips en tricks om de validatie projecten effectiever uit te rollen, te begeleiden of zelfs te leiden. Voor meer details DAG 2 : https://www.co-valent.be/nl/details-formations/?sja=deaeb6f5Zb178Ze911Za96aZ000d3a29f080

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How to Stay Competitive in the Life Sciences Industry? Follow these Market Trends!

As the global life sciences industry continues to flourish, competition among companies is inevitably increasing. To remain competitive, companies need the ability to predict and follow market trends, a feat that can be challenging. But companies can find support in others who are specialized in keeping up with these trends and know how to remain on top of the game.

Join our team

Our trainings

Start2farma: Basis in validatie 1: Equipment & system qualification

November 21 @ 8:30 am – 5:00 pm
GrownInFarma: validatie 2: Equipment & system qualification

November 22 @ 8:30 am – 5:00 pm
Start2farma: BEHANDELEN EN Technische schrijven van deviaties (0 – 2 jaar ervaring)

November 25 @ 8:30 am – 5:00 pm
GLP labo activiteiten binnen GMP life science productiebedrijven

December 2 @ 8:30 am – 5:00 pm
Start2farma: BEHANDELEN EN Technische schrijven van deviaties (0 – 2 jaar ervaring)

December 9 @ 8:30 am – 5:00 pm

About our trainings

Interesting for you?

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